Tunable ultraviolet polarized light switch based on all-dielectric metasurfaces on a stretchable substrate.

Most ultraviolet (UV) passive optics are currently non-tunable and lack external modulation methods because of the poor tunability of wide-bandgap semiconductor materials in UV working media. This study investigates the excitation of magnetic dipole resonances in the solar-blind UV region by hafnium oxide metasurfaces using elastic dielectric polydimethylsiloxane (PDMS). The near-field interactions between the resonant dielectric elements can be modulated by the mechanical strain of the PDMS substrate, which can flatten the structure's resonant peak beyond the solar-blind UV wavelength range, thereby turning on or off the optical switch in the solar-blind UV region. The device has a facile design and can be used in various applications, such as UV polarization modulation, optical communications, and spectroscopy.

Theoretical study on pyrolysis mechanism of decabromodiphenyl ether (BDE-209) using DFT method.

Decabromodiphenyl ether (BDE-209), as a brominated flame retardant (BFR), is widely applied to various consumer products due to its superior performance and affordable pricing to improve the flame resistance of materials. To better comprehend the pyrolysis behavior of BDE-209 and the evolution process of main pyrolysis products, the thermal degradation mechanism of BDE-209 was studied using density functional theory (DFT) method at the theoretical level of M06/cc-pVDZ, and thermodynamic parameters were calculated in this paper. Unimolecular degradation was dominated by cleavage of the ether linkage, which results in a high yield of hexabromobenzene, and fission of the ortho-position C-Br bond is the main competitive reaction channel. In the system of BDE-209 + H, the pyrolysis reaction is majorly characterized by debromination, leading to the formation of considerable HBr and low-brominated diphenyl ethers. Additionally, the hydrogen-derived splitting of the ether bond acts as a mainly competitive channel, which is the source of polybromophenols and polybromobenzenes. The formation of polybrominated dibenzofuran (PBDF) derives from the cyclization reaction of ortho-phenyl-type radicals, which are readily generated through the ortho-position Br atom abstraction by H radical. The formation of polybrominated dibenzo-p-dioxin (PBDD) involves the ortho-C-O coupling reaction of polybromophenoxy radicals, debromination reaction, and cyclization reaction. And the total yield of PBDD/Fs was significantly increased when H was involved. Results presented in this work will provide the helpful information for the treatment and reuse of BDE-209-containing waste plastics through using pyrolysis technology.